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Protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models

OBJECTIVE: The aim of the study was to investigate the protective characteristic of chlorogenic acid, a natural glucosyl xanthone found in Lonicera Japonica on the cerebral ischemia reperfusion injury and the underlying mechanism. METHODS: Focal cerebral ischemia reperfusion model was built by block...

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Autores principales: Miao, Mingsan, Cao, Lihua, Li, Ruiqi, Fang, Xiaoyan, Miao, Yanyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447441/
https://www.ncbi.nlm.nih.gov/pubmed/28579891
http://dx.doi.org/10.1016/j.jsps.2017.04.023
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author Miao, Mingsan
Cao, Lihua
Li, Ruiqi
Fang, Xiaoyan
Miao, Yanyan
author_facet Miao, Mingsan
Cao, Lihua
Li, Ruiqi
Fang, Xiaoyan
Miao, Yanyan
author_sort Miao, Mingsan
collection PubMed
description OBJECTIVE: The aim of the study was to investigate the protective characteristic of chlorogenic acid, a natural glucosyl xanthone found in Lonicera Japonica on the cerebral ischemia reperfusion injury and the underlying mechanism. METHODS: Focal cerebral ischemia reperfusion model was built by blocking the left middle cerebral artery in rats by using the suture-occluded method. Before operation, the corresponding drugs were given for each group once a day for 7 days. After 1 h of final administration, the model was built, after operation, reperfusion was conducted for 22 h, Before the reperfusion 10 min tail vein injection of large, medium and small dose of chlorogenic acid and then mortality was calculated, and Neurological deficit score (NDS) was conducted, and serum was collected to measure the NSE level; a 2 mm thick brain slice located at the intersection of optic nerves was collected for TTC staining, and the percentage of cerebral infarction area was calculated; brain homogenate was collected to measure the ICAM-1, VCAM-1, EPO and HIF-1α levels in brain tissue of cerebral ischemia reperfusion rat models; NGF was detected using immunohistochemical method; the morphological changes in brain tissue was observed with HE staining. RESULTS: All focal cerebral ischemia reperfusion rat models were duplicated successfully. Every chlorogenic acid group with different dosage can significantly reduce the mortality, NDS and cerebral infarction area of rats, and significantly increase the EPO, HIF-1α and NGF levels in brain tissue; significantly improve the pathological lesions of hippocampus and cortex in brain tissue. CONCLUSION: The results showed that chlorogenic acid could protect the focal cerebral ischemia reperfusion injury rat models by adjusting the inflammatory factor, hypoxia factor and nerve growth factor.
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spelling pubmed-54474412017-06-02 Protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models Miao, Mingsan Cao, Lihua Li, Ruiqi Fang, Xiaoyan Miao, Yanyan Saudi Pharm J Original Article OBJECTIVE: The aim of the study was to investigate the protective characteristic of chlorogenic acid, a natural glucosyl xanthone found in Lonicera Japonica on the cerebral ischemia reperfusion injury and the underlying mechanism. METHODS: Focal cerebral ischemia reperfusion model was built by blocking the left middle cerebral artery in rats by using the suture-occluded method. Before operation, the corresponding drugs were given for each group once a day for 7 days. After 1 h of final administration, the model was built, after operation, reperfusion was conducted for 22 h, Before the reperfusion 10 min tail vein injection of large, medium and small dose of chlorogenic acid and then mortality was calculated, and Neurological deficit score (NDS) was conducted, and serum was collected to measure the NSE level; a 2 mm thick brain slice located at the intersection of optic nerves was collected for TTC staining, and the percentage of cerebral infarction area was calculated; brain homogenate was collected to measure the ICAM-1, VCAM-1, EPO and HIF-1α levels in brain tissue of cerebral ischemia reperfusion rat models; NGF was detected using immunohistochemical method; the morphological changes in brain tissue was observed with HE staining. RESULTS: All focal cerebral ischemia reperfusion rat models were duplicated successfully. Every chlorogenic acid group with different dosage can significantly reduce the mortality, NDS and cerebral infarction area of rats, and significantly increase the EPO, HIF-1α and NGF levels in brain tissue; significantly improve the pathological lesions of hippocampus and cortex in brain tissue. CONCLUSION: The results showed that chlorogenic acid could protect the focal cerebral ischemia reperfusion injury rat models by adjusting the inflammatory factor, hypoxia factor and nerve growth factor. Elsevier 2017-05 2017-04-28 /pmc/articles/PMC5447441/ /pubmed/28579891 http://dx.doi.org/10.1016/j.jsps.2017.04.023 Text en © 2017 Production and hosting by Elsevier B.V. on behalf of King Saud University. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Miao, Mingsan
Cao, Lihua
Li, Ruiqi
Fang, Xiaoyan
Miao, Yanyan
Protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models
title Protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models
title_full Protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models
title_fullStr Protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models
title_full_unstemmed Protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models
title_short Protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models
title_sort protective effect of chlorogenic acid on the focal cerebral ischemia reperfusion rat models
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447441/
https://www.ncbi.nlm.nih.gov/pubmed/28579891
http://dx.doi.org/10.1016/j.jsps.2017.04.023
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